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Quinapril Hydrochloride and Hydrochlorothiazide - 54868-2847-1 - (qinapril hydrochloride and hydrochlorothiazide)

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Drug Information of Quinapril Hydrochloride and Hydrochlorothiazide

Product NDC: 54868-2847
Proprietary Name: Quinapril Hydrochloride and Hydrochlorothiazide
Non Proprietary Name: qinapril hydrochloride and hydrochlorothiazide
Active Ingredient(s): 12.5; 20    mg/1; nmol/1 & nbsp;   qinapril hydrochloride and hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Quinapril Hydrochloride and Hydrochlorothiazide

Product NDC: 54868-2847
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078211
Marketing Category: ANDA
Start Marketing Date: 20060803

Package Information of Quinapril Hydrochloride and Hydrochlorothiazide

Package NDC: 54868-2847-1
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-2847-1)

NDC Information of Quinapril Hydrochloride and Hydrochlorothiazide

NDC Code 54868-2847-1
Proprietary Name Quinapril Hydrochloride and Hydrochlorothiazide
Package Description 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-2847-1)
Product NDC 54868-2847
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name qinapril hydrochloride and hydrochlorothiazide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060803
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Strength Number 12.5; 20
Strength Unit mg/1; nmol/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Quinapril Hydrochloride and Hydrochlorothiazide


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